BACKGROUND
[0001] The present invention relates to an aspiration device for use with a smoking article
such as a cigarette for causing the introduction of biologically active materials
into the mouth and respiratory tract of a smoker, in proportion to the amount of smoke
drawn through the smoking article.
BACKGROUND OF THE INVENTION
[0002] It is generally recognized that smoking, particularly cigarette smoking, is a prime
cause of vascular disorders, lung and oral cancer, and cancer of the upper respiratory
tract. It is known that tobacco smoke contains cancer-causing agents and that these
agents are carried to the smoker's mouth and respiratory tract in the tobacco smoke.
It is also known that certain biologically active or drug materials known as biological
response modifiers (BRM), including retinoids (vitamin A and its natural and synthetic
analogs), thymosin, the interferons, and others, have been shown to have the ability
to prevent or modify carcinogen-induced animal and human cancers. These compounds
have the ability not only to modify or inhibit the growth of existing cancers, but
also to block the induction of cancer, i.e., to act as cancer chemopreventive agents.
In addition, a potentially useful method of reducing harmful cigarette smoke inhalation
involves the oral delivery of nicotine from a reduced-smoke or "smokeless" cigarette,
thus satisfying the physiologic need for nicotine while preventing the ingestion of
harmful smoking-related carcinogens and irritants. Furthermore, no general drug delivery
system is presently available which can provide controlled dosages of orally-active
drugs using cigarette smoking as the delivery medium.
[0003] In order to take advantage of the apparent cancer-preventive properties of vitamin
A and its analogs, it has been proposed to provide cigarettes with a filter incorporating
a supply of these materials. In U.S. patent 3,339,558, vitamin A is contained within
a rupturable capsule which is ruptured by the smoker immediately prior to smoking.
U.S. patent 3,525,582 shows a similar cigarette in which vitamin A is encapsulated
in a heat rupturable capsule, which is ruptured by the heat of the burning tobacco.
In U.S. patent 3,667,478, a stabilized form of vitamin A, capable of withstanding
long periods of storage, is distributed throughout the filter, rather than being contained
in a separate capsule. European Patent Application No. 0 003 064 A2 shows a similar
cigarette in which certain synthetic vitamin A analogs are used as the biologic response
modifier.
[0004] In all of the above-mentioned cigarettes, the vitamin A or other BRM or drug is deposited
on the filter material (or the tobacco when no filter is used) adjacent the end of
the cigarette held in the mouth of the smoker. During smoking, the drug is entrained
within the concentrated stream of tobacco smoke passing through the cigarette and
is carried into the mouth of the smoker. The drug is, therefore, exposed within the
cigarette itself to the hot concentrated stream of smoke, creating the possibility
of thermal degradation of the drug substance as well as adverse chemical reactions
with the active ingredients of the tobacco smoke.
SUMMARY OF THE INVENTION
[0005] The above-noted deficiencies of the prior art, wherein a BRM or other drug incorporated
within a cigarette is exposed to the hot concentrated stream of smoke before entering
the smoker's mouth, are obviated by the aspiration device of the present invention,
which provides an elongated container adapted to be positioned within a cigarette
or other smoking article adjacent the end intended to be held in the smoker's mouth.
The container holds a supply of an appropriate BRM or other drug which is aspirated
directly into the smoker's mouth as a result of the suction applied by the smoker
to the end of the cigarette. An air inlet port communicates with the outer surface
of the cigarette and permits air to enter the container in response to the partial
vacuum created by the applied suction. The drug held within the container is discharged
through an exit orifice thereof which is coplanar with the end of the cigarette, so
that mixing of the drug with the tobacco smoke occurs within the mouth of the smoker,
at reduced temperature and lower smoke concentration. By appropriate selection of
the size of the exit orifice from the container, the rate at which the drug is delivered
can be controlled, so that an amount of drug proportional to the amount of smoke withdrawn
from the cigarette or other smoking article can be delivered into the smoker's mouth.
DESCRIPTION OF THE DRAWINGS
[0006] In the attached drawings:
Figure l is a perspective view of the end of a cigarette showing the aspiration device
of the invention as it would typically be installed;
Figure 2 is a section along the line 2-2 of Figure l showing the location and interior
construction of the BRM container of the device;
Figure 3 is a perspective view of a box of cigarettes adapted for holding cigarettes
incorporating the device of the invention; and
Figure 4 is a section along the line 4-4 of Figure 3 showing the filter ends of the
cigarettes within the container of Figure 3.
DETAILED DESCRIPTION
[0007] In a preferred embodiment, the aspiration device l0 of the invention comprises an
elongated container ll having a hollow interior suitable for holding a supply of
a BRM or other drug to be introduced into the mouth and respiratory tract of a smoker
during the act of smoking. As shown in Figure l, aspiration device l0 is installed
in cigarette l2 adjacent the end l3 intended to be inserted into the mouth of the
smoker. Since most cigarettes are provided with filter tips incorporating a wide variety
of filtering media, the device of the invention would most commonly be installed in
a filter tip. It should be understood, however, that the presence of a filter is not
a part of the present invention, which is equally suitable for use in cigarettes
filled entirely with tobacco.
[0008] Aspiration device l0 is contained within an elongated housing l6 of filter tip l4
having an upstream end l7 attached to a conventional cylinder of tobacco l8 within
a paper or similar wrapper l9. The available volume between container ll and housing
l6 is filled with a conventional filter packing 2l, or alternatively with tobacco,
as previously explained.
[0009] The upstream end 22 of container ll is sealed, and adjacent the sealed end is an
inlet port 23 having a bore 24, one end of which communicates with interior of container
ll and the other end of which penetrates the wall of housing l6 to permit the entry
of air into the interior of container ll. The downstream end 26 of con tainer ll,
lying substantially in the same plane as the downstream end of filter tip l4, is provided
with a restricted orifice 27, having an appropriate diameter for controlling the discharge
of any liquid or particulate BRM or other drug contained within the interior of the
container.
[0010] It will be seen that when a smoker draws on the end of a cigarette containing the
device of the invention, a partial suction is created within the interior of the container
ll, causing air to enter through inlet port 23 and to entrain the contents of the
container for discharge through orifice 27 into the smoker's mouth and respiratory
tract. By correlating the diameter of orifice 27 and the viscosity of a liquid drug
composition, or the particle sizes of a particulate drug, the rate at which the drug
is discharged under normal smoking conditions can be adjusted as desired.
[0011] The smoke of the burning cigarette passes through filter packing 2l directly to the
exit end of the cigarette. The walls of container ll serve to protect the drug contents
from being heated by the hot stream of smoke as well as preventing direct contact
with the smoke stream until both the drug and the smoke have exited the end of the
cigarette.
[0012] The material of which container ll is constructed is not critical. Any material
can be used which is inert to the drug contents, resistant to the temperature to which
it is exposed, and easily worked to the desired configuration. Plastic materials,
such as polyethylene and polypropylene, are preferred, because of their low cost,
inertness and ease of fabrication.
[0013] Since the drug contents of the aspiration device may be sensitive to contact with
air or have a tendency to flow out of the device during storage, it is desirable to
provide a closure for the filter end of a cigarette incorporating the device of the
invention. Such a closure can consist of a plastic tape or cup (not shown) sealing
both the open end of inlet port 23 as well as orifice 27.
[0014] A preferred form of commercial package for cigarettes incorporating the device of
the invention, provided with means for sealing the inlet port and exit orifice thereof,
is shown in Figures 3 and 4. Figure 3 shows a conventional "flip-top" box 28 containing
a supply of cigarettes l2 and a base 29 provided with cylindrical openings 3l into
which the filter ends of the cigarettes are inserted. As shown in Figure 4, the openings
3l in base 29 are dimensioned to form a close fit with the ends of the cigarettes,
thereby blocking the inlet ports 23 and orifice 27 of each device against entry of
air or leakage of the BRM contained therein.
[0015] The invention and its use are further illustrated in the following example.
EXAMPLE
[0016] Aspiration devices in accordance with the invention were constructed from polypropylene
plastic tubing having an outer diameter of 2.5 mm, a length of 25 mm and a wall thickness
of 0.5 mm. An inlet port 23 formed from an appropriate length (about 3 mm) of l.5
mm outer diameter polypropylene tubing having an inner diameter of l.0 mm. The end
of container ll adjacent the inlet port was sealed by crimping the tube end with a
heated crimping tool. The volume of each device was 223 microliters. The opposite
end of the device was partially closed by means of a plug having a length of about
2 mm and orifices ranging from 0.56 mm to 0.97 mm in diameter. Each device was placed
within the filter section of a standard l00 mm cigarette with the open ends of the
inlet port and the exit orifice flush with the filter wrapper and the mouth end of
the filter respectively.
[0017] In a series of tests, each container was filled with vitamin A solution (Aquasol
A Drops, Armour Pharmaceutical Co.) which has been mixed with varying proportions
of water to adjust the viscosity and tested in a simulated smoking system in which
sifficient suction was applied to the end of the cigarette to cause a air flow rate
of l L/sec., a rate typical of actual smoking conditions. Two series of runs were
performed, one with an exit orifice diameter of 0.7l mm in the aspiration device and
a second series wherein the orifice had a diameter of 0.9 mm. The time required for
complete emptying of the container was determined.
[0018] The results are summarized in Table l below.

[0019] From an inspection of Table l, it will be seen that at a constant degree of suction,
the flow rate of the liquid BRM out of the dispensing device increased with a decrease
in viscosity of the BRM solution, at a constant exit orifice diameter. The flow rate
similarly increased with an increase in orifice diameter at a constant viscosity.
It is therefore evident that by controlling these two variables (i.e., the viscosity
of the liquid BRM solution, or the exit orifice diameter of the dispensing device),
the rate at which the BRM is introduced into the mouth of the smoker can be controlled,
and made proportional to the rate at which the cigarette is smoked.
[0020] In additional work with the above described aspiration device employing l00% Aquasol
A drops, in which the device was exposed to sufficient suction to produce a flow of
l L/sec. through the cigarette, exit orifice diameters below about 0.5 mm resulted
in no flow of the BRM out of the container. With an orifice diameter of 0.7l mm, the
contents of the device were delivered in 5 simulated puffs (exposure to suction) of
2 seconds duration each. The rate of delivery increased with increasing orifice size,
until at an orifice diameter of about l.0 mm, the entire contents of the device were
delivered in one puff.
[0021] Similar control of the discharge rate from the device can be achieved using a particulate
BRM having mean particle diameters appropriate for depositing the particulate material
within a smoker's respiratory tract and lungs, i.e., ranging from less than 2 to more
than l00 microns in diameter. The size of the outlet orifice diameter can be adjusted
as necessary to control the rate at which the contents of the device of the invention
are delivered when suction is applied to the end of the cigarette.
[0022] Although the device of the invention has been described with particular reference
to use in a cigarette, it will be seen that its use is not so limited. The device
can also be employed with cigars and other smoking articles. In addition, the aspiration
device can be incorporated in a pipe, or a holder for cigarettes or cigars.
[0023] The foregoing detailed description has been given for clearness of understanding
only, and no unnecessary limitations should be understood therefrom.
1. An aspiration device for a smoking article such as a cigarette comprising:
an elongated housing having an axial bore, said housing having an upstream end adapted
to be attached to said smoking article and a downstream exit end through which smoke
drawn by a smoker exits;
a hollow elongated container within said housing having a sealed upstream end, a
downstream exit end which is substantially coplanar with said exit end of said housing,
and an inlet port adjacent its sealed end, said inlet port penetrating said housing
and permitting air to be drawn into said container by said smoker;
said exit end of said container having a restricted orifice through which liquid or
particulate contents of said container are discharged when suction is applied thereto
by said smoker.
2. A device in accordance with claim l wherein any available volume within said housing
not occupied by said container is filled with a filtration medium permeable to smoke.
3. A device in accordance with claim l containing a biologically active composition
within said container.
4. A device in accordance with claim 3 wherein said composition is a solution of
Vitamin A or nicotine.
5. A device in accordance with claim l wherein said restricted orifice has a diameter
of 0.5-l.0 mm.